Mitochondrial DNA depletion syndrome hepatocerebrorenal form 782771007
SNOMED CT code
| SNOMED code | 782771007 |
|---|---|
| name | Mitochondrial DNA depletion syndrome hepatocerebrorenal form |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form (disorder) |
| synonyms |
|
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Finding site | Cerebrum 83678007 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Liver structure 10200004 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Renal tubule structure 58471003 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic renal disease 106000008 Mitochondrial DNA depletion syndrome hepatocerebrorenal form 782771007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Inherited metabolic disorder of nervous system 128190004 Mitochondrial DNA depletion syndrome hepatocerebrorenal form 782771007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic and genetic disorder affecting the liver 235903001 Mitochondrial DNA depletion syndrome hepatocerebrorenal form 782771007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Disorder of pyruvate metabolism and mitochondrial respiratory chain 237981000 Disorder of mitochondrial respiratory chain complexes 237986005 Depletion of mitochondrial DNA 237995002 Mitochondrial DNA depletion syndrome hepatocerebrorenal form 782771007 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Mitochondrial DNA depletion syndrome hepatocerebrorenal form 782771007 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Mitochondrial DNA depletion syndrome hepatocerebrorenal form 782771007 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Disorder of brain 81308009 Mitochondrial DNA depletion syndrome hepatocerebrorenal form 782771007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Mitochondrial DNA depletion syndrome hepatocerebrorenal form 782771007 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Disorder of renal parenchyma 767094002 Renal tubular disorder 95568003 Mitochondrial DNA depletion syndrome hepatocerebrorenal form 782771007 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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